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FDA 510(k)

SUCTION TUBES: HOUSE, BARON

K-Number: K892549 · 1989-05-18

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-05-18
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUCTION TUBES: HOUSE, BARON is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-05-18 under 510(k) number K892549. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION TUBES: HOUSE, BARON?

SUCTION TUBES: HOUSE, BARON is a medical device that received FDA 510(k) clearance on 1989-05-18. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K892549.

When did SUCTION TUBES: HOUSE, BARON receive FDA 510(k) clearance?

SUCTION TUBES: HOUSE, BARON received FDA 510(k) clearance on 1989-05-18, under 510(k) number K892549.

Who is the listed applicant for SUCTION TUBES: HOUSE, BARON?

The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION TUBES: HOUSE, BARON?

The FDA product code for SUCTION TUBES: HOUSE, BARON is GCX.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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Related Devices (Code: GCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K042454STRYKER CASSETTE PUMPStryker EndoscopyK992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMCircon Corp.K972074SUCTION INSTRUMENTATIONWalter Lorenz Surgical, Inc.K971022CHASE SUCKERChase Medical, Inc.K964127MEDI-VAC FLEXI-CLEAR SUCTION HANDLEAllegiance Healthcare Corp.K964519CURITY THORACENTESIS TRAYKendall Healthcare Products Co. Div.Of Tyco Health

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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